2005
DOI: 10.1002/pi.1964
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Synthesis of oligocaprolactone vinyl ether macromonomers and their use for indomethacin encapsulation in polymer nanoparticles based on polycaprolactone macromonomer–maleic anhydride–N‐vinyl pyrrolidone terpolymers

Abstract: International audienceOligocaprolactone macromonomers functionalized with vinyl ether have been synthesized by polymerization of ε-caprolactone in the presence of hydroxy ethyl or butyl vinyl ether and characterised by NMR and Maldi time-of-flight mass spectroscopy. These macromonomers have been copolymerized with maleic anhydride and N-vinyl pyrrolidone to give terpolymers, which have been used to obtain nanoparticles by the phase-separation-dialysis method. Previously dissolving indomethacin in the terpolyme… Show more

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Cited by 17 publications
(24 citation statements)
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“…These approaches can be generally divided into two: dispersion of preformed polymers and polymerization 1,2,3 . A major drawback of nanoparticle preparation by the dispersion of preformed polymers for pharmaceutical purposes is that it requires the use of surfactants to prepare the particles in the aqueous phase, which may generate concerns about toxicity 1 .…”
Section: Introductionmentioning
confidence: 99%
“…These approaches can be generally divided into two: dispersion of preformed polymers and polymerization 1,2,3 . A major drawback of nanoparticle preparation by the dispersion of preformed polymers for pharmaceutical purposes is that it requires the use of surfactants to prepare the particles in the aqueous phase, which may generate concerns about toxicity 1 .…”
Section: Introductionmentioning
confidence: 99%
“…By carefully selecting the initiator systems, PCL functionalized with different end groups have been obtained, such as halogen groups [14,15], double bond [16][17][18], hydroxyl groups [19,20], and silane [21][22][23], which provides a wide range of possibilities for the synthesis of PCL-based copolymers with advanced structures such as block [24][25][26], star-shaped [27,28], comblike [29], brushlike [30], or cross-linked networks [31,32]. Meanwhile, ATRP has been proved to be efficient to synthesize polymer with desired macromolecular architectures [33][34][35][36].…”
Section: Introductionmentioning
confidence: 99%
“…6568 They are approved for use in vivo by the Food and Drug Administration (FDA). 64,69 Their biodegradation by hydrolysis of the ester bond leads to pharmacologically inactive and harmless degradation products, such as lactic acid, glycolic acid, and 6-hydroxycaproic acid from PLA, PGA, and PCL, respectively.…”
Section: Nonviral Carriers For Exogenous Sirna Delivery For Hiv Therapymentioning
confidence: 99%